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Proceedings of the National Academy of Sciences of the United States of America
|
August 20, 2011
Identification and characterization of a functional mitochondrial angiotensin system
Peter M Abadir, D Brian Foster, Michael Crow, et al.
EMBO Molecular Medicine
|
March 16, 2021
Targeted genome editing in vivo corrects a Dmd duplication restoring wild-type dystrophin expression
Eleonora Maino, Daria Wojtal, Sonia L Evagelou, et al.
Environmental Health Perspectives
|
August 17, 2012
The Head-off Environmental Asthma in Louisiana (HEAL) study--methods and study population
Patricia C Chulada, Suzanne Kennedy, Mosanda M Mvula, et al.
Pediatrics
|
July 4, 2006
Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylation
Ronald D Cohn, Erik Eklund, Amanda L Bergner, et al.
Nature Communications
|
August 4, 2015
Clinically relevant copy number variations detected in cerebral palsy
Maryam Oskoui, Matthew J Gazzellone, Bhooma Thiruvahindrapuram, et al.
Nature
|
July 26, 2019
A mutation-independent approach for muscular dystrophy via upregulation of a modifier gene
Dwi U Kemaladewi, Prabhpreet S Bassi, Steven Erwood, et al.
Plos One
|
November 17, 2012
Impaired skeletal muscle regeneration in the absence of fibrosis during hibernation in 13-lined ground squirrels
Eva Andres-Mateos, Rebeca Mejias, Arshia Soleimani, et al.
Environmental Health Perspectives
|
August 17, 2012
Implementation of evidence-based asthma interventions in post-Katrina New Orleans: the Head-off Environmental Asthma in Louisiana (HEAL) study
Herman Mitchell, Richard D Cohn, Jeremy Wildfire, et al.
Contemporary Clinical Trials
|
March 24, 2017
Rationale and study protocol for the Patient-Centered Outcome Aid (PCOA) randomized controlled trial: A personalized decision tool for newly diagnosed ovarian cancer patients
L Wenzel, D Mukamel, K Osann, et al.
BMC Genomics
|
April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome
Christian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Page
of 38
Search research articles
Search
Showing results (331-340 of 379) with videos related to
Sort By:
Page
of 38
Proceedings of the National Academy of Sciences of the United States of America
|
August 20, 2011
Identification and characterization of a functional mitochondrial angiotensin system
Peter M Abadir, D Brian Foster, Michael Crow, et al.
EMBO Molecular Medicine
|
March 16, 2021
Targeted genome editing in vivo corrects a Dmd duplication restoring wild-type dystrophin expression
Eleonora Maino, Daria Wojtal, Sonia L Evagelou, et al.
Environmental Health Perspectives
|
August 17, 2012
The Head-off Environmental Asthma in Louisiana (HEAL) study--methods and study population
Patricia C Chulada, Suzanne Kennedy, Mosanda M Mvula, et al.
Pediatrics
|
July 4, 2006
Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylation
Ronald D Cohn, Erik Eklund, Amanda L Bergner, et al.
Nature Communications
|
August 4, 2015
Clinically relevant copy number variations detected in cerebral palsy
Maryam Oskoui, Matthew J Gazzellone, Bhooma Thiruvahindrapuram, et al.
Nature
|
July 26, 2019
A mutation-independent approach for muscular dystrophy via upregulation of a modifier gene
Dwi U Kemaladewi, Prabhpreet S Bassi, Steven Erwood, et al.
Plos One
|
November 17, 2012
Impaired skeletal muscle regeneration in the absence of fibrosis during hibernation in 13-lined ground squirrels
Eva Andres-Mateos, Rebeca Mejias, Arshia Soleimani, et al.
Environmental Health Perspectives
|
August 17, 2012
Implementation of evidence-based asthma interventions in post-Katrina New Orleans: the Head-off Environmental Asthma in Louisiana (HEAL) study
Herman Mitchell, Richard D Cohn, Jeremy Wildfire, et al.
Contemporary Clinical Trials
|
March 24, 2017
Rationale and study protocol for the Patient-Centered Outcome Aid (PCOA) randomized controlled trial: A personalized decision tool for newly diagnosed ovarian cancer patients
L Wenzel, D Mukamel, K Osann, et al.
BMC Genomics
|
April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome
Christian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Page
of 38